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Evaluating IL-21 as a Potential Therapeutic Target in Crohn's Disease

机译:评估IL-21作为克罗恩病的潜在治疗靶标

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Background and Aim. Interleukin-21 (IL-21) is primarily a T cell-derived cytokine; it is upregulated in patients with Crohn's Disease (CD) and could be a potential new therapeutic target in CD. Methods. In human material, IL-21 and IL-21R expression was investigated by in situ hybridization (ISH) and immunohistochemistry (IHC) in noninflammatory bowel disease (non-IBD) controls and patients with CD. The pathologic role of IL-21 was examined in murine models of T cell-dependent and T cell-independent colitis, either with a neutralizing monoclonal antibody against IL-21 or with the transfer of CD4(+)CD45RB(high)IL-21R(-/-) T cells. Colonic pathology was examined by endoscopy, histopathology, IHC, ELISA, and Luminex. Results. In the human intestine, IL-21 and IL-21R mRNA and protein-expressing cells were observed in the mucosa, in lymphoid aggregates of submucosa in non-IBD controls, and in lymphoid aggregates of muscularis externa in patients with CD. IL-21 expression was most abundant in germinal centers (GCs) of the lymphoid aggregates, and IL-21R expression assessed semiquantitatively, was significantly higher in patients with CD compared to non-IBD controls. Following prophylactic and interventive anti-IL-21 mAb treatment in the adoptive transfer (AdTr) model, clinical and pathological parameters were significantly reduced. The most persistent finding was a reduction in colonic infiltrating neutrophils. As well, Rag2(-/-) mice receiving CD4(+)CD45RB(high)IL-21R(-/-) T cells developed less severe colitis compared to Rag2(-/-) mice receiving CD4(+)CD45RB(high)IL-21R(+/+) T cells. No effect of reduced IL-21 signalling was observed in T cell-independent colitis. Conclusion. Our study shows that patients with CD have significant expression of IL-21 and IL-21R in the gut. As well, we show that neutralization of IL-21 in experimental T cell-driven colitis is associated with a reduction in clinical and pathological findings. This amelioration seems to be associated with a reduction in colon-infiltrating neutrophils.
机译:背景和目标。白细胞介素-21(IL-21)主要是T细胞衍生的细胞因子;克罗恩疾病(CD)患者上调了它,并且可以是CD中的潜在新的治疗靶标。方法。在人体材料中,通过原位杂交(ISH)和免疫组织化学(IHC)在非炎性肠病(非IBD)对照和CD患者中研究了IL-21和IL-21R表达。 IL-21的病理作用在T细胞依赖性和T细胞依赖性结肠炎的鼠模型中检测,具有对IL-21的中和单克隆抗体或CD4(+)CD45RB(高)IL-21R的转移( - / - )T细胞。通过内窥镜检查,组织病理学,IHC,ELISA和Luminex检查结肠病理学。结果。在人肠中,在粘膜中观察在粘膜中的粘膜中的含有IL-21和IL-21R mRNA和蛋白质 - 在非IBD对照中的乳腺癌中,以及CD患者患者肌肉外部的淋巴骨聚集体。 IL-21表达在淋巴聚集体的生发中心(GCS)中最丰富,并且与非IBD对照相比,CD患者分半定量评估的IL-21R表达显着高。在采用转移(ADTR)模型中的预防性和干预抗IL-21 mAb治疗后,临床和病理参数显着降低。最持久的发现是结肠浸润中性粒细胞的降低。同样,接受CD4(+)CD45RB(高)IL-21R( - / - )T细胞的RAG2(/ - / - )小鼠与接受CD4(+)CD45RB的RAG2( - / - )小鼠相比,显着严重的结肠炎(高)IL-21R(+ / +)T细胞。在T细胞无关的结肠炎中没有观察到IL-21信号传导的影响。结论。我们的研究表明,CD患者在肠道中具有显着的IL-21和IL-21R。同样,我们表明在实验性T细胞驱动的结肠炎中的IL-21中和与临床和病理结果的降低有关。这种改善似乎与结肠浸润性嗜中性粒细胞的还原有关。

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